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终末期肝病患者发生肺部真菌感染的危险因素及病原学分析

Risk Factors and Etiology of Pulmonary Fungal Infection in Patients With End-Stage Liver Disease

  • 摘要:
    目的  探讨终末期肝病患者合并肺部真菌感染的危险因素及病原学谱构成。
    方法 对211例终末期肝病患者临床资料进行回顾性分析。根据肺部影像学、临床表现及病原学检测结果,将患者分为3组:肺部真菌感染组(病例组)、肺部非真菌感染组(对照组1)和无肺部感染组(对照组2)。比较病例组与对照组1、对照组2之间临床特征的差异。以无肺部感染患者(对照组2)作为对照,采用单因素和多因素logistic回归分析筛选终末期肝病患者发生肺部真菌感染的独立危险因素,并基于此构建列线图预测模型。
    结果 211例患者中,76例(36.1%)有肺部真菌感染,46例(21.8%)有肺部非真菌感染,89例(42.2%)无肺部感染。多因素logistic回归显示入院时白细胞计数高(OR值=1.211,95%CI:1.011~1.460)、MELD-Na评分高(OR值=1.140,95%CI:1.021~1.282)、合并肝肾综合征(OR值=4.150,95%CI:1.050~17.300)、糖皮质激素累积使用时间超过7 d(OR值=26.832,95%CI:6.361~113.221)及入院时使用高级别抗生素治疗(OR值=6.601,95%CI:1.951~22.362)是肺部真菌感染的独立危险因素。基于上述危险因素构建了命名为TJLFPFI的列线图预测模型,其受试者工作特征曲线下面积为0.899(95%CI:0.853~0.945)。76例肺部真菌感染患者病原学分析显示,痰培养阳性36例(47.4%),痰培养阴性但G试验和(或)GM试验阳性40例(52.6%)。病原学曲霉检出率最高(25/36,59.5%)。
    结论 终末期肝病患者肺部真菌感染与入院时病情严重程度、高级抗生素的早期使用及较长时间糖皮质激素使用相关。曲霉是主要致病菌。TJLFPFI模型在识别高危人群方面有潜在应用价值,预测性能未来仍需进一步验证。

     

    Abstract:
    Objective  To identify the risk factors and investigate etiological spectrum of pulmonary fungal infections (PFIs) in patients with end-stage liver disease (ESLD).
    Methods  A retrospective analysis was performed on the clinical data of 211 ESLD patients. Based on pulmonary imaging, clinical manifestations, and microbiological test results, patients were categorized into three groups, including the PFI group (or the case group), the non-fungal pneumonia group (or the control group 1), and the group without pneumonia (or the control group 2). The clinical characteristics of patients in the the case group were then compared with those of patients in the two control groups. Taking patients without pneumonia as the control, univariate and multivariate logistic regression analyses were performed to identify independent risk factors for PFI, and a nomogram prediction model was constructed based on these risk factors.
    Results  Among the 211 patients, 76 (36.1%) had PFIs, 46 (21.8%) had non-fungal pneumonia, and 89 (42.2%) did not have pneumonia. According to findings from the multivariate logistic regression, elevated white blood cell count upon admission (OR = 1.211; 95% CI, 1.011-1.460), higher Model for End-Stage Liver Disease-Sodium (MELD-Na) score (OR = 1.140; 95% CI, 1.021-1.282), concomitant hepatorenal syndrome (OR = 4.150; 95% CI, 1.050-17.300), cumulative glucocorticoid use for more than seven days (OR = 26.832; 95% CI, 6.361-113.221), and the administration of broad-spectrum antibiotics at the time of hospital admission (OR = 6.601; 95% CI, 1.951-22.362) were identified as independent risk factors for PFI. A predictive nomogram model named TJLFPFI was constructed based on these risk factors. The area under the receiver operating characteristic (AUC) curve of the model was 0.899 (95% CI, 0.853-0.945). Etiologic analysis of the 76 PFI cases revealed that 36 (47.4%) had positive results for culture, while 40 (52.6%) had negative results for sputum culture but tested positive by the 1,3-β-D-glucan test and/or galactomannan test. Aspergillus was the most frequently identified pathogen, detected in 25 of the 36 cases (59.5%).
    Conclusion  PFI in ESLD patients is closely associated with disease severity at admission, early use of broad-spectrum antibiotics, and prolonged glucocorticoid therapy. Aspergillus is the predominant pathogen. The TJLFPFI model shows potential value in identifying high-risk patients, but prospective validation is still warranted.

     

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